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Somatoform Disorders clinical trials

View clinical trials related to Somatoform Disorders.

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NCT ID: NCT01453439 Completed - Anxiety Disorders Clinical Trials

Cognitive-Behavioral Therapy and Supportive Psychotherapy for Body Dysmorphic Disorder

Start date: August 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to learn more about two different types of psychotherapy to help individuals who have body dysmorphic disorder (BDD). BDD is a severe, often chronic, and common disorder consisting of distressing or impairing preoccupation with perceived defects in one's physical appearance. Individuals with BDD have very poor psychosocial functioning and high rates of hospitalization and suicidality. Because BDD differs in important ways from other disorders, psychotherapies for other disorders are not adequate for BDD. Despite BDD's severity, there is no adequately tested psychosocial treatment (psychotherapy) of any type for this disorder. This study will compare the effectiveness of Cognitive Behavioral Therapy and Supportive Psychotherapy as well as predictors of improvement.

NCT ID: NCT01438762 Completed - Clinical trials for Patellofemoral Pain Syndrome

Early Intervention for Adolescents With Patellofemoral Pain Syndrome

Start date: June 2011
Phase: N/A
Study type: Interventional

Self-reported, unspecific knee pain is highly prevalent among adolescents. A large proportion of the unspecific knee pain can be attributed to Patellofemoral Pain Syndrome (PFPS). There are a number of treatment options for PFPS. Physical therapy has been advocated as one of the cornerstones in rehabilitation of patients with PFPS. Twenty-five years ago, McConnell proposed a multimodal approach that combined several treatment options. The regimen included retraining of the vastus medialis oblique muscle through functional weight bearing activities. This exercise is combined with patellar taping, patellar mobilization, and stretching to improve patellar tracking, reduce pain, and enhance vastus medialis oblique muscle activation. Short term results (<12 months) indicates that multimodal physiotherapy is more effective than placebo treatment. While treatment for PFPS may be successful for the short-term, long-term results are less promising. A recent review covering the long term prognosis for patients diagnosed with PFPS, reported that only 1/3 of those diagnosed with PFPS and treated conservatively were pain free 12 months after diagnosis. Further ¼ stopped participating in sports because of knee pain. Predictors of long term outcome (>52weeks) indicate that a long symptom duration, higher age and greater severity at baseline are associated to poorer outcome after treatment. These prognostic factors suggest that an early initiation of treatment might lead to a better long-term prognosis. The purpose of this study is to examine the short and long-term effectiveness of multi-modal physiotherapy compared to standard wait-and-see treatment applied at a very early state of disease among adolescents. The investigators hypothesized a significantly larger proportion of completely recovered patients at three-month follow-up in the interventions group compared to the control group.

NCT ID: NCT01434966 Completed - Clinical trials for Patellofemoral Pain Syndrome

Changes in Quadriceps Function Following Local or Distant Interventions in Individuals With Patellofemoral Pain

Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if interventions applied at a distant site, lumbopelvic region (manipulation and TENS), have a similar effect as interventions applied locally at the knee (TENS) on quadriceps force output and activation as well as reports of pain during common exercises in individuals with PFPS.

NCT ID: NCT01332110 Completed - Clinical trials for Patellofemoral Pain Syndrome

Treatment for Patellofemoral Pain Syndrome Using Footwear

Start date: June 2011
Phase: Phase 1/Phase 2
Study type: Interventional

Patellofemoral pain syndrome (PFPS) is the most common running injury and is believed to be associated with higher than normal knee joint loading. Footwear has been developed that may decrease these knee loads in healthy subjects, but their effects on patients with PFPS are unknown. In this study, we aim to test the effects of such footwear on patients with PFPS. We hypothesize that patients who receive the footwear intervention will show a decrease in knee joint loading, and consequently will show improvements in subjective levels of perceived knee pain over a period of six weeks compared to a control condition.

NCT ID: NCT01290705 Completed - Clinical trials for Patellofemoral Pain Syndrome

Dosage-dependence of Graded Exercise Therapy in Patients With Patellofemoral Pain Syndrome.

Start date: November 2007
Phase: N/A
Study type: Interventional

With this study two different therapeutic exercise regimens will be compared in patients with anterior knee pain (patellofemoral pain syndrome, PFPS).

NCT ID: NCT01250184 Completed - Pain Clinical Trials

Treatment of Myofascial Pain Syndrome With Lidocaine Injection and Physical Therapy.

Start date: May 2009
Phase: Phase 4
Study type: Interventional

Background: Myofascial pain syndrome (MPS) of the shoulder girdle and cervical region is a common musculoskeletal problem that is often chronic or recurrent. It has demonstrated the effectiveness of different treatments such as exercise, injection but not comparing them with each other. The objective of this research was to demonstrate whether lidocaine injection into trigger points combined with a physical therapy program was more effective than each separatetreatment in improving pain, function and quality of life in a group of patients with myofascial pain syndrome (MPS) of the shoulder girdle and cervical region. Design: Single-blind, randomized, controlled clinical trial with three parallel groups in the departments of physical medicine and rehabilitation of two urban hospitals. There were 127 patients with myofascial pain in the shoulder girdle for more than six weeks in length and pain greater than 40 mm on the visual analog scale (VAS). There were three intervention groups: physical therapy (PT), lidocaine injection (LI), or the combination of both (PT + LI). The primary outcome at one month was the VAS, and the secondary outcomes were measured using the SF36 pain scaleat one and three months. Keywords: Myofascial pain, trigger points, lidocaine injection, physical therapy.

NCT ID: NCT01187797 Completed - Depression Clinical Trials

Effects of Emotional Stimulation on the Stress Levels of Healthy Persons

Start date: August 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effects of a short-term emotional stimulation on the mood of healthy persons.

NCT ID: NCT01158430 Completed - Hypochondriasis Clinical Trials

Acceptance and Commitment Group Therapy (ACT) for Patients With Health Anxiety

ACT
Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of Acceptance and Commitment Therapy (ACT) in groups on functional level, emotional problems, and use of health care in patients with severe health anxiety in a randomized, controlled design.

NCT ID: NCT01119469 Completed - Clinical trials for Somatoform Disorders

Comparing Cognitive Therapy and Exposure Therapy in Individuals With Hypochondriasis

Start date: June 2010
Phase: Phase 3
Study type: Interventional

This study will compare the efficacy of cognitive therapy and exposure therapy for treating hypochondriasis.

NCT ID: NCT01106339 Completed - Depression Clinical Trials

Immune Patterns in Pain Patients DSM-IV

IPPPDIV
Start date: August 2007
Phase: N/A
Study type: Observational

The purpose of this study is to define subgroups of patients with somatoform disorders due to DSM-IV by immunological, psychological and genetic characterization.